Come fly with Regal Rexnord and watch your career soar! Join the winning team with a company that offers excellent opportunities to grow your career. Based on experience we will offer $22.00-$30.00/Hr., along with a very competitive benefit package, including 401(k) with a match, that starts day one. We are located in a state of the art, climate-controlled building.Regal Rexnord’s Aerospace and Defense business is on an upward trajectory, we are rapidly growing, and we have opportunities to add new team members. Are you interested in joining a growing team with a fantastic culture that is offering a $4,000 sign-on bonus. Win!Key Accountabilities· Work from process sheets, blueprints, setup sheets, setup cards, machine status boards, and verbal as well as written instructions.· Machine and install or re-cut chuck jaws as required.· Insert and secure tooling in machine turrets and preform machine set ups.· Download and upload programs into machine and make minor programming adjustments as needed.· Operate different types of computerized numerical controls to manufacture a finished machined product by performing a wide range of machining operations within tight tolerances.· Inspect own work for correct dimensions and ensure that company quality and quantity standards are maintained and complete required documentation. Will be required to inspect the work of other machinists.· May be required to operate multiple machines and rotating departments.· Enters data into ERP system.· Load and unload component piece parts with weights up to 25 lbs· Other duties as assigned.Qualifications“Restrictions imposed by federal export control laws may limit this job opportunity to candidates who are a ‘U.S. Person’, which includes U.S. citizens, U.S. nationals, U.S. permanent residents, individuals granted asylum in the United States, and refugees in the United States, or who otherwise can qualify for a license that permits them to hold the position.”· Previous experience and demonstrated proficiency in operating CNC lathe, CNC mill machines, or resistance spot welder (any combination of two machines), with intermediate knowledge and experience with setting up machines.· Requires a high school education or equivalent experience.· Must be reliable with minimal call-offs during the year, we value and expect good attendance· Minimum of 2 years of related experience, and knowledge of machining principles and methods for computer numerical controlled machine tools required· Demonstrated ability to perform basic mathematical calculations.· Must be able to read and interpret work instructions and blueprints in English.· External candidates will be required to pass a Machinist test which measures mechanical aptitude.RewardsMatching 401(k) contributionMedical/Dental/Vision InsuranceShort-Term and Long-Term Disability InsuranceAccidental Death and Dismemberment InsuranceFlexible Spending Accounts (Medical and Dependent Care) & Health Savings AccountsCritical illness and Accident Insurance, as well as Life Insurance, and an EAPEducational ReimbursementHow To ApplyInternal Associates must sign into career site www.regalrexnord.com, click Login, enter Username and Password then apply and upload a current resume. Regal Rexnord associates must be in good standing for consideration for job openings. This includes satisfactory or above ratings in job performance and no corrective actions, PIP’s, disciplinary issues or warnings in the last 12 months.Equal Employment Opportunity Employer:Female/Sexual Orientation/Gender Identity/Minority/Veteran/DisabledBenefitsMedical, Dental, Vision and Prescription Drug CoverageSpending accounts (HSA, Health Care FSA and Dependent Care FSA)Paid Time Off and Holidays401k Retirement Plan with Matching Employer ContributionsLife and Accidental Death & Dismemberment (AD&D) InsurancePaid LeavesTuition AssistanceAbout Regal RexnordRegal Rexnord is a $6.5B publicly held global industrial manufacturer with 30,000 associates around the world who help create a better tomorrow by providing sustainable solutions that power, transmit and control motion. The Company’s electric motors and air moving subsystems provide the power to create motion. A portfolio of highly engineered power transmission components and subsystems efficiently transmits motion to power industrial applications. The Company’s automation offering, comprised of controls, actuators, drives, and precision motors, controls motion in applications ranging from factory automation to precision control in surgical tools.The Company’s end markets benefit from meaningful secular demand tailwinds, and include factory automation, food & beverage, aerospace, medical, data center, warehouse, alternative energy, residential and commercial buildings, general industrial, construction, metals and mining, and agriculture.Regal Rexnord is comprised of three operating segments: Industrial Powertrain Solutions, Power Efficiency Solutions, and Automation & Motion Control. Regal Rexnord has offices and manufacturing, sales and service facilities worldwide. For more information, including a copy of our Sustainability Report, visit RegalRexnord.com.Equal Employment Opportunity StatementRegal Rexnord is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex/gender, sexual orientation, gender identity, age, ancestry, national origin, marital status, citizenship status (unless required by the applicable law or government contract), disability or protected veteran status or any other status or characteristic protected by law. Regal Rexnord is committed to a diverse and inclusive workforce. We are committed to building a team that represents diverse and inclusive backgrounds, perspectives, and skills. If you’d like to view a copy of the company’s affirmative action plan or policy statement, please email . If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail .Equal Employment Opportunity PostersNotification to Agencies: Please note that Regal Rexnord Corporation and its affiliates and subsidiaries ("Regal Rexnord") do not accept unsolicited resumes or calls from third-party recruiters or employment agencies. In the absence of a signed Master Service Agreement or similar contract and approval from HR to submit resumes for a specific requisition, Regal Rexnord will not consider or approve payment to any third-parties for hires made.

Dover is a diversified global manufacturer with annual revenue of over $8 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Clean Energy & Fueling, Imaging & Identification, Pumps & Process Solutions and Climate & Sustainable Technologies. Dover combines global scale with operational agility to lead the markets we serve. Recognized for our entrepreneurial approach for over 60 years, our team of approximately 24,000 employees takes an ownership mindset, collaborating with customers to redefine what's possible. Headquartered in Downers Grove, Illinois, Dover trades on the New York Stock Exchange under "DOV." Additional information is available at dovercorporation.com. Position Summary: Reporting directly to the Dover Director of Advanced Manufacturing Machining, the Advanced Manufacturing Machining Engineer is responsible for executing the manufacturing roadmap for optimizing machining processes, proper use of the equipment, design specifications, setup reviews, and new control strategies. AMME is responsible to lead and ensure that new equipment purchases are specified, sourced, qualified, and properly transitioned into mass production, meeting Dover and customer requirements and timing.Essential Duties and Responsibilities:Support and partner with OpCo to drive improving OEE through initiatives such as SMED, TPM, etc. for new and existing equipment. Work on Dover corporate strategy to work with OpCo to drive productivity by internalizing spend (Buy2Make) on new capex and existing equipment by maximizing machine utilization. Lead SMED Events - Lead Site CNC technology Assessments – Project Manage Site improvement activitiesSupport and partner with OpCo to support on maturity journey for the Machining Excellence Playbook. Provide technical development and deployment for new technologies related to machining to drive productivity improvements.Drive and support machining strategy on productivity improvement by maximizing asset utilization.Assist in the evolution of the equipment and perform acceptance evaluation accordingly.Identify, recommend, procure, and install machine shop equipment as well as ensure all equipment is thoroughly maintained and calibratedSupport workforce utilization, space requirements, workflow, and design layout of equipment and workspace for maximum efficiency.Continuously improve, provide recommendation on upgrade of equipment to maximize asset utilization.Interface with tooling supplier to ensure use of proper tooling for production. Work with suppliers to develop better cutting tools for specific PM applications.Develop machining capability in-house while making changes to enhance the machine functionality.Identify, develop, and deploy new machining methods (or refine existing) to improve quality, reduce cost, and optimize build scheduleUtilize lean manufacturing methodology for process development and problem solvingPerform root cause analyses when non-conformances are identified and deploy corrective actionsHelping and supporting manufacturing, to achieve safety, quality, efficiency and throughput goals, identifying opportunities to improve.Apply Project Management skills & tools to lead and support capital equipment/improvement projects.Investigate equipment performance and identify any problems for corrective actions and solutions.Writes/revises User Requirement Specs, Functional Requirement, Design Specs, Qualifications, etc.Supports Factory and Site Acceptance Tests, Machinability Studies, and validation protocols.Responsible for review and approve PFMEA, DFMEA, PPAPs, and Standard Operating Procedures SOP and ensure that manufacturing and operations comply with. Utilize continuous improvement methodology to improve internal processes.Must be able to interact constructively across the whole organization to identify issues and implement improvements.Hands-on support of new products and new process launches.Must be able to handle multiple projects and multiple priorities simultaneously.Travel up to 70% may be required. Ability to perform other duties as assigned.Qualifications/Requirements/Desired Characteristics:Bachelor’s degree in mechanical, electrical, or manufacturing engineering, industrial technology, or equivalent mix of education and experience.Minimum five (5) years’ experience in manufacturing engineering directly working with machining processes.Experience setting up and operating state-of-the-art machining equipment.Extensive experience in machining and maintenance. Well-versed in standard machine shop manufacturing processes and setupsStrong experience with SolidWorks or another mechanical CAD systemHighly experienced with a variety of precision conventional and advanced metrology systems (photogrammetry, CMMs, 3D imaging)Strong commitment to proper safety precautions in design and practiceStrong understanding of Lean concepts.Excellent interpersonal and influencing skills to interact with other departments.Ability to multi-task and perform in a dynamic environmentStrong sense of urgency, accountability and highly objective orientedHighly organized and efficient in approaching tasks, a self-starter with the ability to problem-solve.Clear, concise, and articulate communication skills - verbal, written, and listening.Strong team player, work ethic, and commitment to win the right way.Strong analytical skills, ability to think big, act small, and scale fast.Key Accomplishments – Previous 12 MonthsDemonstrated experience in successfully achieving machining startups.Proven experience developing/starting new manufacturing processesDemonstrated experience improving productivity by machining optimizationDemonstrated experience improving OEE. And proven reduction in unplanned maintenance hoursDemonstrated experience utilizing Advanced Product Quality Planning Methodology and the integrated product and process development techniques within it. (e.g., Process Flow Diagrams, PFMEA, Control Plans, I/PPAP, Standard Work).Proven success managing medium and large-scale projects from concept development through successful implementation.Work Arrangement : Hybrid Salary Range : - We consider several job-related, non-discriminatory factors when determining the pay rate for a position, including, but not limited to, the position’s responsibilities, a candidate’s work experience, a candidate’s education/training, the position’s location, and the key skills needed for the position. Pay is one of the Total Rewards that we provide to compensate and recognize employees for their work.All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law.Job Function : Engineering#LI-JR1

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Our MissionAt Lilly we unite caring with discovery to create medicines that make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.ResponsibilitiesThe Parenteral (PAR) Operators (Entry to Expert roles) will support start up activities at Eli Lilly’s newly acquired Kenosha County site. This role is required to bring the area into service which may include formulation, aseptic isolator barrier filling, and equipment preparation. They will become the experts within their assigned area and educate their team in the proper operation of the facility. This position may require travel (2-4 week trips and/or 3-12 month short term assignments) domestically with the opportunity for travel internationally to collaborate, train with, and learn from sites who currently produce our medicines.After project phase is complete, this role will be responsible for ensuring continuous supply of our medicines by; expertly running the process, troubleshooting, and collaborating cross-functionally, and holding all to our safety first/quality always mindset. Operators will support daily activities to meet capacity plans while developing their own and our team’s capabilities.As a site leader and expert at our growing site, you’ll have significant opportunities for growth into future leadership and technical roles.Key Objectives/Deliverables: IntegrityProvide leadership on manufacturing floor ensuring high level of safety, quality, and productivity to maintain reliable supply of products to patients.Responsible for maintaining a safe work environment, exemplifying safe working practices, and being accountable for supporting HSE goals.Act as both administrator and technical leaders for operations. Set a good example through demonstrated knowledge of procedures, compliance with quality systems, and teaching of proper techniques.ExcellenceTechnical leader:Key resource for troubleshooting and functions as the primary point of contact for issue escalation on the production floor.Responsible for administering technical training and ensuring all operators are trained to perform tasks.Operate the equipment and perform activities as required to meet production schedule.Assists in checking execution documentation (Electronic Batch Record, SAP, Cleaning Logs)Drives key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.Respect for PeopleSupport Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes and controls for the PAR areas.Key liaison between operations and support functions.Basic QualificationsWe have several levels open for Operator which are based on the experience and education you bring.Minimum education: High School Diploma or GEDAbility to effectively communicate (electronically, written and verbal)Flexibility - the ability to troubleshoot and triage challengesComputer proficiency (desktop software, MS office).Time Commitments and Work AuthorizationMust Pass a “fitness for duty” physical examShift flexibilityAbility to work overtime as required.Ability to wear safety equipment (glasses, shoes, gloves, etc)Ability to work and gown in a cleanroom (Grade C, ISO 8) environment.Ability to participate in professional development opportunitiesDepending on the candidate’s experience, the position may require a short-term assignment of 3-12 months domestically or internationally to train and be certified on existing processes and establish global contacts.Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.Additional Skills/ PreferencesExperience with, completion of, or understanding of:Leadership and the ability to train/educate team members.STEM degree or certificationsAseptic filling, single use assemblies, isolator technology.Automated, semi-automated, and/or manual inspection.Knowledge of current Good Manufacturing Practices (CGMPs)Experience in operations or manufacturing environments.Pharmaceutical, medical device or food processing industriesManufacturing Execution Systems and electronic batch release.Continuous improvement (Lean, Six Sigma methodologies)Highly automated equipment (inspection, packaging, filling, assembly, etc)SAP, Electronic Batch RecordsThis job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. This position requires flexibility and a commitment to meeting operational needs, which may involve working irregular hours or shifts, including swing shifts. The ability to adapt to various schedules and provide coverage as needed is essential for maintaining continuous production and supporting our team's objectives. Your dedication to meeting these scheduling requirements will contribute significantly to the success of our operations and the quality of our products. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.#WeAreLilly

COMPANY OVERVIEWAs the nation's largest producer of clean, carbon-free energy, Constellation is a company purposely-built to meet the challenges of the climate crisis. Constellation has been the leader in clean energy production for more than a decade and we are growing our company and capabilities. Now, we're accelerating, speeding our low-carbon or no-carbon power to more people in more places, day and night, providing our customers and communities with options to buy, manage and use energy as part of their decarbonization mission. The race is on to confront the climate crisis and Constellation is ready to meet the challenge. Come join us as we lead energy, together.TOTAL REWARDSConstellation offers a wide range of benefits and rewards, designed to help our employees thrive professionally and personally. In addition to highly competitive salaries, we offer a bonus program, 401(k) with company match, employee stock purchase program comprehensive medical, dental and vision benefits, including a robust wellness program paid time off for vacation, holidays and sick days and much more.Salary range will fall in the $132,000 - 147,000 range, depending upon experience. The senior individual in Constellation Projects and Services responsible for the departments Quality Assurance and Quality Control (QA/QC) Program. Regular interfacing with Industry code committees related to identification and resolution of QA program issues. Oversee inspection activities performed by supplemental Quality Verification (QV) support personnel assigned to the site for inspections involving major modifications / projects. Oversee work performed by equipment vendors. Manage day-to-day QV inspections to comply with company and code requirements and commitments. Prioritize and communicate quality and non-conformance issues to senior management, craft and their supervision to assure issue resolution. Document the results of inspection activities as required by company policies.Primary Duties and AccountabilitiesResponsible and accountable for the governance of the QA/QC Program and communicating/identifying program or implementation weaknesses as necessary to maintain department&rsquos performance.Provides governance, oversight, and support in development and implementation of the Constellation Projects and Services Business Plan, Budget, Management Model and Procedures.Communicate and escalate significant quality issues to appropriate levels of management.Maintains industry knowledge of current codes and standards to effectively prepare and conduct the QA program reviews and evaluations.Reviews commercial contract terms as they relate to Contractor QC programs and reviews contractor and subcontractor QA programs in accordance with Constellation&rsquos QA/QC program requirements.Reviews commissioning and test plans in accordance with current codes and standardsManages QA personnel schedules and priorities, when necessary.Manage QV inspection activities to comply with company requirements. Document the results of inspection activities in accordance with Constellation&rsquos management model.Works with subject matter experts (SME&rsquos) in the development of critical QC hold points and assist scheduler/planner in integrating hold points into the project schedule.Managing of engineering disposition workflow as it relates to non-conformance requests and test result reviews.Interface with preferred vendors to coordinate procurement of contracted inspector resources.Provide oversight of supplemental QV inspectors in accordance with department requirements and expectations.Oversees and verifies accuracy of As-Build documentation submittals and coordinates review with appropriate stake holders.Oversee major equipment vendor production activities and document inspection results in accordance with Constellation&rsquos management model.Minimum QualificationsFour-year college degree and 10+ years professional experience with exceptional performanceProfessional level power plant experience, transmission and distribution or utility substation experienceDemonstrated ability to interface with craft and management and clearly communicate issuesDemonstrated ability to read civil, electrical, and structural drawingsExcellent Computer Skills professional-level experienceAbility to travel to project locations and equipment vendors. Minimum travel requirement is 25% Current or previously certified quality inspectorPrevious equipment inspection experienceFamiliarity with relay protection systems, documentation, settings, and data system monitoring architecturePrevious supervisory experience in Operations, Maintenance / craft, Work Control, Engineering or Supply Management

The Production Supervisor is responsible for leading a team of manufacturing operators and assisting with the manufacture of pharmaceutical products while following cGMP protocol and ensuring a safe, quality, reliable, compliant and cost-efficient operation.Responsibilities:• Controls production activities, material flow, and inventory to achieve cost and quality targets and production schedules of assigned production line(s)• Supervises activities of production operators to assure safe, efficient manufacture of quality products in accordance with policy and procedures• Coordinates with Maintenance, Engineering, Quality Control and Quality Assurance to assure and improve cGMP compliance• Manages daily scheduling of employees to ensure lines are staffed with appropriate manpower• Monitors, reviews and completes manufacturing procedures and log books• Ensures that manufacturing area and equipment are in satisfactory condition• Oversees continuous improvement activities and visual control boardsQualifications:• Bachelor's Degree with a minimum 3 years' progressive experience in a manufacturing environment.OR• GED or High School Diploma plus 7-10 years of manufacturing experience. Union environment preferred.• Prior supervisory experience or experience leading groups is strongly preferred.• Experience working in a GMP controlled environment preferred.• Pharmaceutical Industry experience preferred. • Six Sigma / Lean Manufacturing skills a plus. • Adaptability to change and to perform under pressure with time constraints. • Demonstrated Leadership skills – experience in leading a high performing manufacturing team in a fast paced, regulated, discrete batch environment. • Strong Communication skills – Ability to clearly communicate, both verbally and in writing, to all levels of the organization.Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.Our BenefitsCSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.Please take the time to review our benefits site to see what’s available to you as a CSL employee.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Behring!

Dover is a diversified global manufacturer with annual revenue of over $8 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Clean Energy & Fueling, Imaging & Identification, Pumps & Process Solutions and Climate & Sustainable Technologies. Dover combines global scale with operational agility to lead the markets we serve. Recognized for our entrepreneurial approach for over 60 years, our team of approximately 24,000 employees takes an ownership mindset, collaborating with customers to redefine what's possible. Headquartered in Downers Grove, Illinois, Dover trades on the New York Stock Exchange under "DOV." Additional information is available at dovercorporation.com. Position Summary: Reporting directly to the Dover Director of Advanced Manufacturing Machining, the Advanced Manufacturing Machining Engineer is responsible for executing the manufacturing roadmap for optimizing machining processes, proper use of the equipment, design specifications, setup reviews, and new control strategies. AMME is responsible to lead and ensure that new equipment purchases are specified, sourced, qualified, and properly transitioned into mass production, meeting Dover and customer requirements and timing.Essential Duties and Responsibilities:Support and partner with OpCo to drive improving OEE through initiatives such as SMED, TPM, etc. for new and existing equipment. Work on Dover corporate strategy to work with OpCo to drive productivity by internalizing spend (Buy2Make) on new capex and existing equipment by maximizing machine utilization. Lead SMED Events - Lead Site CNC technology Assessments – Project Manage Site improvement activitiesSupport and partner with OpCo to support on maturity journey for the Machining Excellence Playbook. Provide technical development and deployment for new technologies related to machining to drive productivity improvements.Drive and support machining strategy on productivity improvement by maximizing asset utilization.Assist in the evolution of the equipment and perform acceptance evaluation accordingly.Identify, recommend, procure, and install machine shop equipment as well as ensure all equipment is thoroughly maintained and calibratedSupport workforce utilization, space requirements, workflow, and design layout of equipment and workspace for maximum efficiency.Continuously improve, provide recommendation on upgrade of equipment to maximize asset utilization.Interface with tooling supplier to ensure use of proper tooling for production. Work with suppliers to develop better cutting tools for specific PM applications.Develop machining capability in-house while making changes to enhance the machine functionality.Identify, develop, and deploy new machining methods (or refine existing) to improve quality, reduce cost, and optimize build scheduleUtilize lean manufacturing methodology for process development and problem solvingPerform root cause analyses when non-conformances are identified and deploy corrective actionsHelping and supporting manufacturing, to achieve safety, quality, efficiency and throughput goals, identifying opportunities to improve.Apply Project Management skills & tools to lead and support capital equipment/improvement projects.Investigate equipment performance and identify any problems for corrective actions and solutions.Writes/revises User Requirement Specs, Functional Requirement, Design Specs, Qualifications, etc.Supports Factory and Site Acceptance Tests, Machinability Studies, and validation protocols.Responsible for review and approve PFMEA, DFMEA, PPAPs, and Standard Operating Procedures SOP and ensure that manufacturing and operations comply with. Utilize continuous improvement methodology to improve internal processes.Must be able to interact constructively across the whole organization to identify issues and implement improvements.Hands-on support of new products and new process launches.Must be able to handle multiple projects and multiple priorities simultaneously.Travel up to 70% may be required. Ability to perform other duties as assigned.Qualifications/Requirements/Desired Characteristics:Bachelor’s degree in mechanical, electrical, or manufacturing engineering, industrial technology, or equivalent mix of education and experience.Minimum five (5) years’ experience in manufacturing engineering directly working with machining processes.Experience setting up and operating state-of-the-art machining equipment.Extensive experience in machining and maintenance. Well-versed in standard machine shop manufacturing processes and setupsStrong experience with SolidWorks or another mechanical CAD systemHighly experienced with a variety of precision conventional and advanced metrology systems (photogrammetry, CMMs, 3D imaging)Strong commitment to proper safety precautions in design and practiceStrong understanding of Lean concepts.Excellent interpersonal and influencing skills to interact with other departments.Ability to multi-task and perform in a dynamic environmentStrong sense of urgency, accountability and highly objective orientedHighly organized and efficient in approaching tasks, a self-starter with the ability to problem-solve.Clear, concise, and articulate communication skills - verbal, written, and listening.Strong team player, work ethic, and commitment to win the right way.Strong analytical skills, ability to think big, act small, and scale fast.Key Accomplishments – Previous 12 MonthsDemonstrated experience in successfully achieving machining startups.Proven experience developing/starting new manufacturing processesDemonstrated experience improving productivity by machining optimizationDemonstrated experience improving OEE. And proven reduction in unplanned maintenance hoursDemonstrated experience utilizing Advanced Product Quality Planning Methodology and the integrated product and process development techniques within it. (e.g., Process Flow Diagrams, PFMEA, Control Plans, I/PPAP, Standard Work).Proven success managing medium and large-scale projects from concept development through successful implementation.Work Arrangement : Hybrid Salary Range : - We consider several job-related, non-discriminatory factors when determining the pay rate for a position, including, but not limited to, the position’s responsibilities, a candidate’s work experience, a candidate’s education/training, the position’s location, and the key skills needed for the position. Pay is one of the Total Rewards that we provide to compensate and recognize employees for their work.All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law.Job Function : Engineering#LI-JR1

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Our MissionAt Lilly we unite caring with discovery to create medicines that make life better for people around the world.We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.ResponsibilitiesThe Parenteral (PAR) Operators (Entry to Expert roles) will support start up activities at Eli Lilly’s newly acquired Kenosha County site. This role is required to bring the area into service which may include formulation, aseptic isolator barrier filling, and equipment preparation. They will become the experts within their assigned area and educate their team in the proper operation of the facility. This position may require travel (2-4 week trips and/or 3-12 month short term assignments) domestically with the opportunity for travel internationally to collaborate, train with, and learn from sites who currently produce our medicines.After project phase is complete, this role will be responsible for ensuring continuous supply of our medicines by; expertly running the process, troubleshooting, and collaborating cross-functionally, and holding all to our safety first/quality always mindset. Operators will support daily activities to meet capacity plans while developing their own and our team’s capabilities.As a site leader and expert at our growing site, you’ll have significant opportunities for growth into future leadership and technical roles.Key Objectives/Deliverables: IntegrityProvide leadership on manufacturing floor ensuring high level of safety, quality, and productivity to maintain reliable supply of products to patients.Responsible for maintaining a safe work environment, exemplifying safe working practices, and being accountable for supporting HSE goals.Act as both administrator and technical leaders for operations. Set a good example through demonstrated knowledge of procedures, compliance with quality systems, and teaching of proper techniques.ExcellenceTechnical leader:Key resource for troubleshooting and functions as the primary point of contact for issue escalation on the production floor.Responsible for administering technical training and ensuring all operators are trained to perform tasks.Operate the equipment and perform activities as required to meet production schedule.Assists in checking execution documentation (Electronic Batch Record, SAP, Cleaning Logs)Drives key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.Respect for PeopleSupport Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes and controls for the PAR areas.Key liaison between operations and support functions.Basic QualificationsWe have several levels open for Operator which are based on the experience and education you bring.Minimum education: High School Diploma or GEDAbility to effectively communicate (electronically, written and verbal)Flexibility - the ability to troubleshoot and triage challengesComputer proficiency (desktop software, MS office).Time Commitments and Work AuthorizationMust Pass a “fitness for duty” physical examThis position will be expected to work 2nd shift (6pm-6am) on a rotating 2-2-3 schedule once fully trained.Ability to work overtime as requiredAbility to wear safety equipment (glasses, shoes, gloves, etc)Ability to work and gown in a cleanroom (Grade C, ISO 8) environment.Ability to participate in professional development opportunitiesDepending on the candidate’s experience, the position may require a short-term assignment of 3-12 months domestically or internationally to train and be certified on existing processes and establish global contacts.Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.Additional Skills/ PreferencesExperience with, completion of, or understanding of:Leadership and the ability to train/educate team members.STEM degree or certificationsAseptic filling, single use assemblies, isolator technology.Automated, semi-automated, and/or manual inspection.Knowledge of current Good Manufacturing Practices (CGMPs)Experience in operations or manufacturing environments.Pharmaceutical, medical device or food processing industriesManufacturing Execution Systems and electronic batch release.Continuous improvement (Lean, Six Sigma methodologies)Highly automated equipment (inspection, packaging, filling, assembly, etc)SAP, Electronic Batch RecordsThis job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. This position requires flexibility and a commitment to meeting operational needs, which may involve working irregular hours or shifts, including swing shifts. The ability to adapt to various schedules and provide coverage as needed is essential for maintaining continuous production and supporting our team's objectives. Your dedication to meeting these scheduling requirements will contribute significantly to the success of our operations and the quality of our products. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.#WeAreLilly

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Position Brand Description:The Manufacturing Operator will work in the Kenosha County (pleasant Prairie) Parenteral Manufacturing site where Parenteral products for domestic and international markets are manufactured and packaged. The primary purpose of the position is to safely inspect high quality pharmaceutical products utilizing Lilly standards by following good manufacturing practices in controlled facilities. Additionally, the position will require the operation of various automated and semi-automated equipment in manufacturing areas as well as performing manual inspections. The operator will focus on inspecting these high-quality medicines by abiding by the Lilly culture of integrity, excellence, and respect for people.This position will require travel (2–8-week trips and/or 3–4-month short term assignments) domestically to collaborate, train with, and learn from sites who currently produce our medicines.Key Objectives / Deliverables:Adhere to Parenteral Plant safety policies and procedures; contribute to a safe work environment.Setup and operations in non-aseptic manufacturing processes, including the set up, use, and/or operation of automated and semi-automated inspection machines in controlled facilities.Adherence to standard operating procedures, current Good Manufacturing Practices, and safety policies / procedures.Document process steps on appropriate batch documentation (paper and electronic).Participate in department meetings, team building, and training activities.Providing input for department SOPs and training.Minimum Requirements:Experience working in a manufacturing environment.Must pass a post offer physical exam.Must pass eye exam and not be color blind.Authorization to work in the United States without employment visa sponsorship.Additional Preferences:Experience with GMPs.Ability to work through production issues including basic troubleshooting skills, and use of tools.PMX, Flow-stream or other electronic batch documentation system knowledge.Previous pharmaceutical manufacturing experience.Manual, automated, and semi-automated inspection experience.Strong attention to detail in carrying out of manufacturing conduct and technique, and performing and documenting all production activities on paper and on computer based systems.Basic math skills, including the evaluation of the results of this data.Basic computer skills, including the use of HMIs and other computer terminals used to monitor equipment status, document production activities, the capability to learn in more detail.Excellent documentation skills.Proven team work skills in working closely with an operational team in the setup, running, and changeover of a manufacturing line.Responsible for maintaining a safe work environment, working safely, and accountable for supporting all Health and Safety Corporate and site goals.Education Requirements:High school diploma or equivalent.Other Information: Some of the products in Parenteral Operations are known allergens, and consequently, a post offer allergy exam may be required.Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc).Must be willing to work overtime, weekends, and off shifts when required.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.#WeAreLilly

Description: Milton Hershey School (MHS) is one of the world's best private schools, where students in pre-K through 12th grade from disadvantaged backgrounds receive an exceptional career-focused education with housing, meals, and moreand all costs are covered. Thanks to the generosity of Milton and Catherine Hershey, who founded the school in 1909, the school is fully endowed and has the resources to ensure both students and staff are provided everything they need to thrive. MHS is hiring married couples to become flex houseparents. Flex houseparents are couples who reside in on-campus student homes, guiding and nurturing a group of approximately 8-12 students. Flex houseparents provide a consistent family-like structure for students and handle responsibilities such as driving, administering medication, budgeting, reporting, etc. When initially hired, flex houseparents cover different student homes before being assigned to one specific home. Benefits ·Salary of $43,825 per person (a total compensation package of approx. $150,000 per couple which includes free housing, meals while on duty, utilities, and more) ·Comprehensive benefits: medical, dental, and vision insurance; health savings and flexible spending accounts; life insurance; disability options; retirement savings ·Relocation assistance and paid training provided ·Schedule of nine days on followed by three days off. Workdays include a period of personal time while students are at school ·Three-week paid summer vacationQualifications: ·Experience working or volunteering with youth, preferably from under-served settings ·This is a two-person job for couples who have been legally married for at least two years ·Both spouses should be age 27 or older ·No more than three dependent children may reside in the student home ·Abide by a smoke-free and weapon-free campus. No alcohol is permitted while on duty ·Limitations on pets. Only fish and one dog of approved breeds is permitted ·Valid driver’s license; ability to become certified to drive student home vans ·Couples must be comfortable leading students in daily devotions and take students to Judeo-Christian Sunday chapel services (Note: Proselytizing is prohibited) ·High school diploma or GED required ·Must be able to lift up to 50 lbs. ·Candidates must demonstrate a high degree of integrity as all staff are role models for students. ·Both spouses must complete an individual employment application This is a unique career path that takes consideration and commitment from both spouses. If you have any specific questions before or after applying, please reach out to our recruitment team at .

Description: Milton Hershey School (MHS) is one of the world's best private schools, where students in pre-K through 12th grade from disadvantaged backgrounds receive an exceptional career-focused education with housing, meals, and moreand all costs are covered. Thanks to the generosity of Milton and Catherine Hershey, who founded the school in 1909, the school is fully endowed and has the resources to ensure both students and staff are provided everything they need to thrive. MHS is hiring married couples to become flex houseparents. Flex houseparents are couples who reside in on-campus student homes, guiding and nurturing a group of approximately 8-12 students. Flex houseparents provide a consistent family-like structure for students and handle responsibilities such as driving, administering medication, budgeting, reporting, etc. When initially hired, flex houseparents cover different student homes before being assigned to one specific home. Benefits ·Salary of $43,825 per person (a total compensation package of approx. $150,000 per couple which includes free housing, meals while on duty, utilities, and more) ·Comprehensive benefits: medical, dental, and vision insurance; health savings and flexible spending accounts; life insurance; disability options; retirement savings ·Relocation assistance and paid training provided ·Schedule of nine days on followed by three days off. Workdays include a period of personal time while students are at school ·Three-week paid summer vacationQualifications: ·Experience working or volunteering with youth, preferably from under-served settings ·This is a two-person job for couples who have been legally married for at least two years ·Both spouses should be age 27 or older ·No more than three dependent children may reside in the student home ·Abide by a smoke-free and weapon-free campus. No alcohol is permitted while on duty ·Limitations on pets. Only fish and one dog of approved breeds is permitted ·Valid driver’s license; ability to become certified to drive student home vans ·Couples must be comfortable leading students in daily devotions and take students to Judeo-Christian Sunday chapel services (Note: Proselytizing is prohibited) ·High school diploma or GED required ·Must be able to lift up to 50 lbs. ·Candidates must demonstrate a high degree of integrity as all staff are role models for students. ·Both spouses must complete an individual employment application This is a unique career path that takes consideration and commitment from both spouses. If you have any specific questions before or after applying, please reach out to our recruitment team at .